To develop stable and efficient silver(I) catalysts and evaluate the role of sulfur and phosphorus donor ligands in the catalytic cycloaddition of selected organic azides and alkynes (AAC), a series of mononuclear Ag(I) and heteronuclear Ag(I)-Fe(II) complexes were synthesized. The synthesis utilized phosphine and sulfur donors from the dialkyldithiophosphate and borate families, specifically Na[SH2B(mt)]. These complexes are designated as [(dppf)AgSP(S)(OPr)] (1), [SHB(mt)Ag(μ-dppf)AgSHB(mt)] (2), [(dppf)Ag(μ-dppf)Ag(dppf)] (3), and [(dppe)AgSHB(mt)] (5). The complexes 1-5 were characterized using a combination of H, C{H}, and P{H} NMR spectroscopy, as well as IR spectroscopy techniques. In two instances, single-crystal X-ray diffraction analysis was also employed. Complex 3 exhibited high catalytic activity and regioselectivity in the cycloaddition reaction conducted in water at 40 °C.
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http://dx.doi.org/10.1039/d4dt02825b | DOI Listing |
Dalton Trans
November 2024
Department of Chemistry, Institute for Advanced Studies in Basic Sciences (IASBS), 444 Prof. Sobouti Blvd., Gava Zang, Zanjan 45137-66731, Iran.
To develop stable and efficient silver(I) catalysts and evaluate the role of sulfur and phosphorus donor ligands in the catalytic cycloaddition of selected organic azides and alkynes (AAC), a series of mononuclear Ag(I) and heteronuclear Ag(I)-Fe(II) complexes were synthesized. The synthesis utilized phosphine and sulfur donors from the dialkyldithiophosphate and borate families, specifically Na[SH2B(mt)]. These complexes are designated as [(dppf)AgSP(S)(OPr)] (1), [SHB(mt)Ag(μ-dppf)AgSHB(mt)] (2), [(dppf)Ag(μ-dppf)Ag(dppf)] (3), and [(dppe)AgSHB(mt)] (5).
View Article and Find Full Text PDFSmall
October 2024
Fraunhofer Institute for Environmental, Safety and Energy Technology UMSICHT, Osterfelderstraße 3, 46047, Oberhausen, Germany.
In recent years, CO electrolysis, particularly the electrochemical reduction of CO to CO in zero-gap systems, has gained significant attention. While Ag-coated gas diffusion electrodes are commonly used in state-of-the-art systems, heterogenized molecular catalysts like bis-coordinated homoleptic silver(I) N,N-bis(arylimino)-acenaphthene (Ag-BIAN) complexes are emerging as a promising alternative due to their tunability and high mass activity. In this study, the influence of ink composition on the performance of Ag-BIAN-based GDEs in zero-gap electrolyzers (ZGEs) are systematically explored at 60 °C and 600 mA cm⁻.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
October 2024
The Soft2D Lab, State Key Laboratory of Metal Matrix Composites, Shanghai Key Laboratory of Electrical Insulation and Thermal Ageing, School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, 130 Dongchuan Road, Shanghai, 200240, China.
Metal-organic frameworks (MOFs) have been widely studied due to their versatile applications and easily tunable structures. However, heteroatom-metal coordination dominates the MOFs community, and the rational synthesis of carbon-metal coordination-based MOFs remains a significant challenge. Herein, two-dimensional (2D) MOFs based on silver-carbon linkages are synthesized through the coordination between silver(I) salt and isocyanide-based monomers at ambient condition.
View Article and Find Full Text PDFOrg Lett
June 2024
College of Pharmaceutical Sciences, Ritsumeikan University, Kusatsu 525-8577, Shiga, Japan.
α-Fluorinated aryl esters pose a challenge in synthesis via -arylation of α-fluorinated carboxylates owing to their low reactivities. This limitation has been addressed by combining a silver catalyst with aryl(trimethoxyphenyl)iodonium tosylates to access α-fluorinated aryl esters. We envision that the catalytic system involves high-valent aryl silver species generated via the oxidation of silver(I) salt.
View Article and Find Full Text PDFJ Am Chem Soc
June 2024
School of Chemistry, University of Bristol, Cantock's Close, Bristol, BS8 1TS, United Kingdom.
Monofluoroalkenes are stable and lipophilic amide bioisosteres used in medicinal chemistry. However, efficient and stereoselective methods for synthesizing -monofluoroalkenes are underdeveloped. We envisage β-fluoro-vinyl iodonium salts (-FVIs) as coupling partners for the diverse and stereoselective synthesis of -monofluoroalkenes.
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